Cladotanytarsus Kieffer (Diptera: Chironomidae): several distinctive species reviewed on the basis of records from Canada and USA
Author
Puchalski, Mateusz
Author
Giłka, Wojciech
text
Zootaxa
2017
4242
2
344
358
journal article
36303
10.11646/zootaxa.4242.2.7
8632c8ac-22fd-42bc-b95c-820c0c029c20
1175-5326
376427
8511A4B8-D82F-49EE-9132-E941B4C5D2C4
Cladotanytarsus bilyji
Giłka
et
Puchalski
,
sp. nov.
(
Figs 2
,
3
)
Type
material.
Holotype
, adult male:
CANADA
,
MANITOBA
,
Lake Winnipeg
,
Old Fishing Dock
(
51°33’ N
/
96°43’ W
),
16 June 1971
, leg.
E. Johnson
&
M. Roberts
(prep.
O.A. Saether
)
.
Paratype
:
USA
.
OHIO
.
Clermont County
,
Shayler Run
at
Baldwin Road
(
39°07’06” N
/
84°12’59” W
),
20 September 1999
,
1 adult
male, leg.
J. Trybula. Ex
coll.
M. & J.E. Sublette
. Deposit in DEUM.
Derivatio nominis.
The specific epithet honours Bohdan Bilyj (Etobicoke,
Canada
), to commemorate his contribution to the study of Nearctic
Cladotanytarsus
.
Diagnosis.
Anal point strongly elongate, evenly tapering toward apex. Superior volsella slender, narrowed at mid length, with field of microtrichia on basal part dorsally. Stem of median volsella
ca.
40 µm long, longer than its setiform and 7–8 furcate lamellae, all arranged evenly on median and apical part of stem. Inferior volsella with lateral knee-like extension at base, with well-developed angular dorsomedian ridge.
FIGURE 2.
Cladotanytarsus bilyji
Giłka
et
Puchalski
,
sp. nov.
, male. Wing.
Description
.
Adult male
(n = 2).
Colouration
(slide-mounted specimens). Eyes black. Antennal pedicel, tentorium, scutal stripes, scutellum, postnotum and sternum dark brown. Head capsule, antennal flagellum, mouthparts and abdomen greenish to light brown; hypopygium and legs slightly darker. Wing membrane transparent with greenish undertone, veins brownish.
Head
. Eyes reniform, broadly separated. Antenna with 13 flagellomeres, AR 0.92–0.94; plume fullydeveloped. Frontal tubercles cylindrical, 12–24 µm long. Lengths of palpomeres 2–5 (in µm): 32–36, 84–104, 100– 108, 164 (n = 1). Clypeus semicircular, with 14–15 setae.
Thorax chaetotaxy
. Ac 7–8, Dc 8, Pa 1, Scts 4–6.
Wing
(
Fig. 2
). Length 1520–1720 µm. Shape, venation pattern and chaetotaxy typical of the genus, as shown in
Fig. 2
; Cu1, R1 and m3+4 bare or with few macrotrichia at most; VR Cu 1.18–1.28.
Legs
. Fore leg tibia with straight spur
ca.
20 µm long. Combs of mid and hind leg tibiae separated, each bearing straight spur:
ca.
15–20 µm long on mid leg and up to
ca.
30 µm long on hind leg. Basitarsus of mid leg with 2–4 hook-shaped sensilla chaetica. For lengths of leg segments and leg ratios, see
Table 2
.
TABLE 2.
Leg segment lengths (µm) and leg ratios of male
Cladotanytarsus bilyji
sp. nov.
(n = 1 when segments missing or deformed).
fe |
Ti |
ta1 |
ta2 |
ta3 |
ta4 |
ta5 |
LR |
p1 |
627–715 |
369 |
731 |
398 |
399 |
221 |
111 |
1.98 |
p2 |
649–900 |
472–642 |
288–295 |
162–192 |
118–140 |
66–73 |
52–70 |
0.46–0.61 |
p3 |
704–826 |
915–964 |
450 |
288 |
244 |
155 |
103 |
0.65 |
Hypopygium
(
Fig. 3
). Gonostylus shorter than gonocoxite,
ca.
70 µm long, with blunt apex. Anal tergite with V-type separated bands and 7–8 median setae placed in two rows. Anal point elongate, evenly tapering towards slender apex (slightly deformed in
paratype
specimen,
Fig. 3
C), bearing 7–8 spinulae between well-developed crests, entire area surrounding base of anal point covered with microtrichia (
Fig. 3
A, C). Superior volsella slender, elongate, more or less narrowed at mid length, bearing field of microtrichia dorsally only on basal part or proximal 1/3 at most, 6–11 dorsal setae, 1–2 setae on anteromedian margin and 3 long setae placed on conical tubercles at base. Digitus curved, long, extending far beyond superior volsella, with finger-like tip (
Fig. 3
A, D). Stem of median volsella slightly curved and directed posteriorly, long (
ca.
40 µm), bearing several setiform and 7–8 furcate lamellae: 4 strong and 3–4 weaker, all arranged evenly on median and apical part of stem (
Fig. 3
B, E). Inferior volsella with lateral knee-like extension at base, evenly curved and directed posteromedially, darkly pigmented dorsomedian ridge distinctly protruding, angular (
Fig. 3
A, B, F).
FIGURE 3.
Cladotanytarsus bilyji
Giłka
et
Puchalski
,
sp. nov.
, male.
A
,
B
—hypopygium in dorsal (A) and ventral aspect (B) (holotype);
C
—anal point (variation, paratype);
D
—superior volsella and digitus (variation);
E
—median volsella (holotype);
F
—inferior volsella (paratype) (D—magnified
ca.
2 times relative to A; E, F—magnified
ca.
3 times relative to A).
Remarks.
Apart from the strongly elongate anal tergite point, this new species can be distinguished from other
Cladotanytarsus
on the following combination of characters: the superior volsella slender and narrowed at mid length, with field of microtrichia only on basal part dorsally, the median volsella composed of a long stem and 7–8 furcate lamellae and the inferior volsella with a lateral knee-like extension at the base, bearing a well-developed angular dorsomedian ridge.
According to preliminary determinations (Sublette, Saether; pers. comm.), there are at least 8 or 9 additional
Cladotanytarsus
species recorded from the Lake Winnipeg region (
locus typicus
of
C. bilyji
), which should be compared with those described by
Bilyj and Davies (1989)
from northwestern
Ontario
. We examined all the
Cladotanytarsus
species by Bilyj (
op. cit.
) known from adult males (excl.
C. aeiparthenus
Bilyj, 1989
). However, even when atypical variations are included, most of the males examined (except for
C. muricatus
Bilyj, 1989
, see remarks below) do not fully fit the present concept of the strongly elongate and narrow hypopygial anal point. Males of those species have relatively short anal points (
C. daviesi
Bilyj, 1989
,
C. pinnaticornis
Bilyj, 1989
), without a distinct distal elongation and/or at least distinctly broadened at the base. Males of
C. elaensis
Bilyj, 1989
have acute anal points, but are relatively broad and surrounded with a microtrichia-free area at the base; in
C. tribelus
Bilyj, 1989
the anal point is narrow and parallel-sided but moderately long (
Bilyj & Davies 1989; figs 6, 8
). As far as the general shape of the anal point is concerned, there is a slight resemblance between the males of
C. fusiformis
Bilyj, 1989
and those of
C. bilyji
; although these two species can be easily separated also by the shape of the superior volsella, which in the former is nearly half as long as the digitus, and the median volsella has a smaller number of lamellae (
cf.
Fig. 3
and
Bilyj & Davies 1989
, fig. 4). Originally,
C. fusiformis
was also compared with
C. nigrovittatus
(
Goetghebuer, 1922
)
. The latter species is presumed to be the closest relative of
C. bilyji
(see the key below). Finally, the males of
C. mancus
(Walker, 1856)
[or the
C. mancus
group
sensu
Giłka (2001)
], often misidentified with
C. nigrovittatus
, should also be included in this comparison. They differ in the length proportions of the median volsella stem-lamellae (the stem longer relative to its lamellae in
C. bilyji
), the number of lamellae (greater in
C. bilyji
), and the arrangement of median setae on the anal tergite (dispersed in
C. mancus
).